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Diseases
Genes (860)
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APOB
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
ABHD5
Cerebral Creatine Deficiency
TTPA
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia
LIPA
Acid Lipase Disease
Hypercholesterolemia
GAMT
Guanidinoacetate Methyltransferase Deficiency
LDLR
Hypercholesterolemia
Cystinosis
ABCC9
Cantú Syndrome
PQBP1
Renpenning's Syndrome
MYLK
Hypercholesterolemia
Berdon Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
RHBDF2
Howel–evans Syndrome
KCNJ8
Cantú Syndrome
Enamel-Renal Syndrome
IFIH1
Singleton Merten Syndrome
APOE
Hypercholesterolemia
PCSK9
Hypercholesterolemia
CYP7A1
Hypercholesterolemia
LPL
Hypercholesterolemia
APOA1
Cerebral Creatine Deficiency
Familial Isolated Vitamin E Deficiency
Hypercholesterolemia